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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764526Generated: October 31, 2026

Benzoyl chloride → HCID 22768412, compound

https://huagongshe.com/reaction/1764526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Chloro-2-hydrazinyl-5-phenyl-3H-1,4-benzodiazepineHCID 12390874—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22768412HCID 22768412—

Reaction Steps

To a solution of 1.4 parts of 7-chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine, prepared in Example 1, in 25 parts by volume of tetrahydrofuran is added 0.62 part by volume of benzoyl chloride, and the mixture is stirred at room temperature for 2 hours to complete the reaction. The reaction mixture is neutralized with a saturated aqueous solution of sodium bicarbonate. The resulting white precipitate is separated, washed with water and then with methanol, and dried, whereby 2-(2-benzoylhydrazino)-7-chloro-5-phenyl-3H-1,4-benzodiazepine is yielded as crystals. Recrystallization from a mixture of chloroform and methanol yields white needles melting at 207° C to 208° C (effervescence).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116956
Source datasetuspto-grants-1978_09
ORD IDord-c06c7db227304bc590742438d1764b2a
Source noteuspto-grants-1978_09